Ionic Interactions 1971
DOI: 10.1016/b978-0-12-553001-9.50006-2
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Equilibrium Properties of Ionized Dilute Electrolytes

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Cited by 63 publications
(51 citation statements)
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“…(52), which in turn can be interpreted as the probability of finding two oppositely charged ions at the separation r. The minimum then correspond to a liminal between bound and unbound configurations. A much more careful analysis of the dipolar partition function has been carried out by Falkenhagen and Ebeling based on the resummed virial expansion [19]. They found that that the low temperature expansion of the Bjerrum equilibrium constant is identical to the equilibrium constant which can be constructed on the basis of the resummed virial expansion.…”
Section: The Bjerrum Associationmentioning
confidence: 99%
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“…(52), which in turn can be interpreted as the probability of finding two oppositely charged ions at the separation r. The minimum then correspond to a liminal between bound and unbound configurations. A much more careful analysis of the dipolar partition function has been carried out by Falkenhagen and Ebeling based on the resummed virial expansion [19]. They found that that the low temperature expansion of the Bjerrum equilibrium constant is identical to the equilibrium constant which can be constructed on the basis of the resummed virial expansion.…”
Section: The Bjerrum Associationmentioning
confidence: 99%
“…One way of doing this, while preserving the linearity of the theory, is to postulate existence of dipoles whose concentration is governed by the law of mass action. In the leadingorder approximation the dipoles can be treated as ideal noninteracting specie [17,18,19]. The total number of particles N = ρV is then subdivided into monopoles N 1 = ρ 1 V and dipoles N 2 = ρ 2 V .…”
Section: The Bjerrum Associationmentioning
confidence: 99%
“…This process can be treated as a reversible chemical reaction, say, (+) + (−) ⇀ ↽ (+, −), leading to equilibrium densities of free ions and dipoles, varying with T and ρ 1,16 . In a continuum model, however, there arises a serious question as to precisely what configurations are to be considered as bound pairs 16,32,33 . In practice, this relates directly to the problem of determining the proper association constant K(T ).…”
Section: B Bjerrum Ion Pairingmentioning
confidence: 99%
“…The simplest theory of correlations is the random phase approximation (RPA), which is equivalent to a one-loop expansion around the mean-field solution (or the saddle-point) [15,16]. Corrections due to the strongcoupling limit effects can be incorporated into the RPA framework by an explicit incorporation of Bjerrum pairs, which are dimers between particles of opposite species [1,2,6,17,18]. For the primitive model this procedure correctly shifts the critical point of a gas-liquid transition to higher densities.…”
Section: Introductionmentioning
confidence: 99%